Canonical Allele Identifier: CA2611933829
Gene: LSP1 HGNC NCBI

Linked Data

gnomAD v4: 11-1852881-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1852881C>T , CM000673.2:g.1852881C>T GRCh38
NC_000011.9:g.1874111C>T , CM000673.1:g.1874111C>T GRCh37
NC_000011.8:g.1830687C>T NCBI36
NG_011509.1:g.4912C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000676039.1:c.-192-72C>T ENSP00000502383.1:n.-192-72C>T